Mauricio J. De Castro Pretelt
Medical Genetics | Pediatrics
900 Ne 10th St
Ouhp Family Medicine
Oklahoma City, OK 73104
Ouhp Family Medicine
Oklahoma City, OK 73104
Last Updated: 09/26/2026
Save publications for later
Sign Up
Not sure about your diagnosis?
Check Your Symptoms
Found 21 publications
Challenges in Interpretation and Reporting of Gross, Histologic, and Genetic Autopsy Findings: The Importance of Postmortem Genetic Testing and Multidisciplinary Teams.
Journal: The American journal of forensic medicine and pathology
Published: June 05, 2025
Comparing the clinical utility of pharmacogenomic genotyping and next generation sequencing in a military health system adult medicine clinic.
Journal: Pharmacogenomics
Published: February 21, 2025
A Multidisciplinary Approach to Navigating Variants of Uncertain Significance in Sudden Infant Deaths: A Case Report of 2 Siblings With an SCN10A VUS.
Journal: The American journal of forensic medicine and pathology
Published: January 02, 2025
Biochemical signatures of disease severity in multiple sulfatase deficiency.
Journal: Journal of inherited metabolic disease
Published: July 03, 2023
Assessing Clinical Utility of Pharmacogenetic Testing in the Military Health System.
Journal: Military medicine
Published: February 17, 2023
Points to consider in the practice of postmortem genetic testing: A statement of the American College of Medical Genetics and Genomics (ACMG).
Journal: Genetics in medicine : official journal of the American College of Medical Genetics
Published: January 10, 2023
Points to consider in the detection of germline structural variants using next-generation sequencing: A statement of the American College of Medical Genetics and Genomics (ACMG).
Journal: Genetics in medicine : official journal of the American College of Medical Genetics
Published: September 26, 2022
Precision Medicine-A Demand Signal for Genomics Education.
Journal: Military medicine
Published: March 08, 2021
Airmen and health-care providers' attitudes toward the use of genomic sequencing in the US Air Force: findings from the MilSeq Project.
Journal: Genetics in medicine : official journal of the American College of Medical Genetics
Published: June 07, 2020
Natural history of multiple sulfatase deficiency: Retrospective phenotyping and functional variant analysis to characterize an ultra-rare disease.
Journal: Journal of inherited metabolic disease
Published: March 31, 2020
Automated typing of red blood cell and platelet antigens from whole exome sequences.
Journal: Transfusion
Published: May 09, 2019
Correction to: Manifesting heterozygotes in McArdle disease: a myth or a reality-role of statins.
Journal: Journal of inherited metabolic disease
Published: July 22, 2018
Last Updated: 09/26/2026